ArticleFrontiers in microbiology2025
The single-cell transcriptional landscape of lung cells from PCV2d-infected mice.
Article in Frontiers in microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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Who cites it
3 citing papers in PubMed.
- Single-cell analysis reveals an endothelial TP53-CXCL14 axis in breast cancer progression.Journal of translational medicine · 2026Article
- CCL chemokines as prognostic and immunotherapeutic markers in prostate cancer: a comprehensive analysis.World journal of surgical oncology · 2026Article
- Spatial transcriptomic profiling of porcine tissue microarray detecting subclinical circovirus infection.Frontiers in veterinary science · 2026Article
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Authors and funding
10 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Introduction: Porcine Circovirus (PCV2) infection is prevalent in pig farming and causes significant economic losses. In recent years, the PCV2d subtype has become the most prevalent genotype worldwide, exhibiting higher virulence, leading to more severe viremia and organ damage. Therefore, studying the biological characteristics of the PCV2d subtype is of great significance. Methods: We established a PCV2d infection model using BALB/c mice and employed single-cell RNA sequencing (scRNA-seq) to systematically analyze the transcriptome of 10 cell types in the lung tissues of infected mice. We developed a comprehensive marker gene catalog for these cell types. Results: Compared to uninfected mice, PCV2d infection induced extensive viral replication and immunosuppressive responses in most cell types. Monocyte macrophages with high levels of viral replication, pro-inflammatory cytokines, and various cell population interactions occurring through CD40-CD40L and CXCL14-CXCR4 were identified. These cells predominantly mediate antigen presentation and processing pathways Discussion: Our data uncovered a complex unique immune response scenario in the lung tissue of mice after PCV2d infection, deciphering the potential mechanisms underlying PCV2d-driven inflammatory responses in mice. Furthermore, this study provides a rich database for the molecular basis of different cell types' responses to PCV2d infection.
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